Canonical Allele Identifier: CA269648943

Gene: DLL4

Linked Data

• dbSNP Id: rs958091296
• gnomAD v3: 15-40931922-T-C
• gnomAD v4: 15-40931922-T-C
• MyVariant Identifiers: chr15:g.41224120T>C (hg19) ; chr15:g.40931922T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40931922T>C , CM000677.2:g.40931922T>C	GRCh38
NC_000015.9:g.41224120T>C , CM000677.1:g.41224120T>C	GRCh37
NC_000015.8:g.39011412T>C	NCBI36
NG_046974.1:g.7590T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000249749.7:c.658+156T>C MANE Select	ENSP00000249749.5:n.658+156T>C
ENST00000249749.6:c.658+156T>C	ENSP00000249749.5:n.658+156T>C
ENST00000559440.1:n.887+156T>C
NM_019074.3:c.658+156T>C	NP_061947.1:n.658+156T>C
NM_019074.4:c.658+156T>C MANE Select	NP_061947.1:n.658+156T>C